Lower-Limb Vibratory Sense Decreased: Causes & Reasons

Possible Causes for Lower-Limb Vibratory Sense Decreased

Autosomal Dominant Spastic Paraplegia Type 6

limbs Decreased lower limb vibratory sense Decreased vibratory sense in lower limbs Decreased vibratory sense in the lower extremities Decreased vibratory sense in the lower [rarediseases.info.nih.gov]

[…] sensation Decreased vibration sense Decreased vibratory sense Diminished vibratory sense Impaired vibratory sense [ more ] 0002495 Lower limb hyperreflexia Overactive lower [rarediseases.info.nih.gov]

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Insidious onset Gradual onset 0003587 Lower limb muscle weakness Lower extremity weakness Lower limb weakness [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 10

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Knee clonus 0011449 Pes cavus High-arched foot 0001761 Progressive Worsens with time 0003676 Spastic gait [rarediseases.info.nih.gov]

[…] who have these symptoms is not available through HPO Autosomal dominant inheritance 0000006 Hyperreflexia Increased reflexes 0001347 Impaired vibration sensation in the lower [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 4

sense in lower limbs Decreased vibratory sense in the lower extremities Decreased vibratory sense in the lower limbs Diminished vibratory sensation in the legs [ more ] 0002166 [rarediseases.info.nih.gov]

[…] sensation in extremities 0002936 Hyperreflexia Increased reflexes 0001347 Impaired vibration sensation in the lower limbs Decreased lower limb vibratory sense Decreased vibratory [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 17

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Insidious onset Gradual onset 0003587 Low back pain 0003419 Memory impairment Forgetfulness Memory loss [rarediseases.info.nih.gov]

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Lower limb muscle weakness Lower extremity weakness Lower limb weakness Muscle weakness in lower limbs [ [rarediseases.info.nih.gov]

Spinocerebellar Ataxia Type 23

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Neuronal loss in central nervous system Loss of brain cells 0002529 Polyneuropathy Peripheral nerve disease [rarediseases.info.nih.gov]

[…] available through HPO Autosomal dominant inheritance 0000006 Cerebellar atrophy Degeneration of cerebellum 0001272 CNS demyelination 0007305 Impaired vibration sensation in the lower [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 8

Symptoms include hyperreflexia, extensor plantar responses, degeneration of the lateral corticospinal tracts, decreased vibratory sense in the lower limbs, pes cavus and atrophy [cags.org.ae]

limb spasticity and weakness. [cags.org.ae]

[…] primarily affecting the central nervous system Mode of Inheritance Autosomal dominant Gene Map Locus Spastic paraplegia 8 is a neurologic disorder characterized by severe lower [cags.org.ae]

Autosomal Dominant Spastic Paraplegia Type 19

limb spasticity and weakness. [cags.org.ae]

[…] primarily affecting the central nervous system Mode of Inheritance Autosomal dominant Gene Map Locus Spastic paraplegia 8 is a neurologic disorder characterized by severe lower [cags.org.ae]

Autosomal Recessive Spastic Paraplegia Type 7

Clinical features of the disease include lower limb spasticity and weakness, spastic ataxic gait, hyperreflexia, extensor plantar responses, pyramidal signs, decreased vibratory [link.springer.com]

sense in the lower limbs, degeneration of the lateral corticospinal tracts, cerebral white matter lesions, dysarthria, cognitive and memory deficits, cortical atrophy, and [link.springer.com]

Most affected individuals have proximal or generalized weakness in the legs and impaired vibration sense. Onset is mostly in adulthood (ranging from 11 to 72 years). [link.springer.com]

Autosomal Dominant Spastic Paraplegia Type 13

limb spasticity and weakness. [cags.org.ae]

[…] primarily affecting the central nervous system Mode of Inheritance Autosomal dominant Gene Map Locus Spastic paraplegia 8 is a neurologic disorder characterized by severe lower [cags.org.ae]

Spastic Paraplegia - Ataxia - Mental Retardation

limb spasticity; Lower limb weakness; Spastic gait; Hyperreflexia; Extensor plantar responses; Ataxia; Dystonia; Dysarthria; Mental retardation ; Decreased vibratory sense [findzebra.com]

[…] in lower limbs; Cerebellar atrophy; Patellar and ankle clonus MISCELLANEOUS: Highly variable phenotype CAMOS syndrome is characterised by the association of a non-progressive [findzebra.com]

NECK: [Eyes]; Abnormal extraocular movements GENITOURINARY: [Bladder]; Urinary urgency; Urinary incontinence; Sphincter disturbances NEUROLOGIC: [Central nervous system]; Lower [findzebra.com]

Spinal Cord Compression

Consultant Radiation Oncologist Published on Oct 26, 2013 Malignant Spinal Cord Compression(Metstatic aspects in detail) 1. Maliganant Spinal Cord Compression Dr Sasikumar Sambasivam Dept. Of Palliative Medicine 2. Intra medullary Intradural Extramedullary Extradural Compressive Myelopathy Compressive Myelopathy 3.[…] [slideshare.net]

Autosomal Dominant Spastic Paraplegia Type 36

Chad A. Noggle, Raymond S. Dean, Arthur MacNeill Horton Springer Publishing Company, 2012 - 804 Seiten I am pleased to include this text in my library, and I am confident that it will serve as an excellent resource for years to come."-- PsycCRITIQUES This book serves as an A-Z reference that addresses the[…] [books.google.de]

Autosomal Dominant Spastic Paraplegia Type 12

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Autosomal Dominant Spastic Paraplegia Type 29

[…] urinary tract 0010936 Clonus 0002169 Hyperreflexia in upper limbs 0007350 Impaired vibratory sensation Decreased vibration sense Decreased vibratory sense Diminished vibratory [rarediseases.info.nih.gov]

Myelocerebellar Disorder

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Variable expressivity 0003828 Showing of 28 | Last updated: 5/1/2019 If you need medical advice, you can [rarediseases.info.nih.gov]

[…] who have these symptoms is not available through HPO Ankle clonus Abnormal rhythmic movements of ankle 0011448 Autosomal dominant inheritance 0000006 Babinski sign 0003487 Decreased [rarediseases.info.nih.gov]

Autosomal Recessive Spastic Paraplegia Type 46

Showing of 36 | 80%-99% of people have these symptoms Babinski sign 0003487 Impaired vibratory sensation Decreased vibration sense Decreased vibratory sense Diminished vibratory [rarediseases.info.nih.gov]

[…] sense Impaired vibratory sense [ more ] 0002495 Lower limb muscle weakness Lower extremity weakness Lower limb weakness Muscle weakness in lower limbs [ more ] 0007340 Spastic [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 38

Disease Ontology : 12 A hereditary spastic paraplegia that has material basis in variation in the chromosome region 4p16-p15. MalaCards based summary : Spastic Paraplegia 38, Autosomal Dominant, also known as spg38, is related to spastic paraplegia 10. An important gene associated with Spastic Paraplegia 38, Autosomal[…] [malacards.org]

Autosomal Recessive Spastic Paraplegia Type 11

Advanced Search Help Advanced search lets you search selected properties of the classification. You could search all properties or a selected subset only First, you need to provide keywords in the Search Text field then check the properties that you'd like to include in the search. The system will search for the[…] [icd.who.int]

Autosomal Recessive Spastic Ataxia Type Charlevoix-Saguenay

A 39-year-old man with long-standing ataxia, spasticity, dysarthria, and peripheral neuropathy was found to have diffuse thickening of the retinal nerve fiber layer in both eyes, as manifested by prominent retinal striations and confirmed by optical coherence tomography. Magnetic resonance imaging showed severe[…] [ncbi.nlm.nih.gov]

Autosomal Recessive Spastic Paraplegia Type 5A

Panel de precisión de paraplejia espástica hereditaria La paraplejía espástica hereditaria (HSP) incluye un grupo de enfermedades familiares que se caracterizan por la degeneración progresiva de los tractos corticoespinales responsables del movimiento y la sensación. Las HSP se diferencian en formas «puras» si hay[…] [igenomix.es]

Autosomal Dominant Optic Atrophy - Hearing Loss - Peripheral Neuropathy Syndrome

Información en español Title Other Names: Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy; OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY; DOMINANT OPTIC ATROPHY PLUS SYNDROME; Dominant optic atrophy, deafness, ptosis, ophthalmoplegia,[…] [rarediseases.info.nih.gov]

Autosomal Dominant Spastic Paraplegia Type 37

limb weakness and spasticity, sphincter dysfunction, decreased vibratory sense at the ankles and with additional manifestations including optical neuropathy, nystagmus, strabismus [rarediseases.info.nih.gov]

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Lower limb hyperreflexia Overactive lower leg reflex 0002395 Lower limb hypertonia 0006895 Lower limb muscle [rarediseases.info.nih.gov]

Spinocerebellar Ataxia

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Pain insensitivity 0007021 Pes cavus High-arched foot 0001761 Sensorimotor neuropathy Nerve damage causing [rarediseases.info.nih.gov]

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Neuronal loss in central nervous system Loss of brain cells 0002529 Polyneuropathy Peripheral nerve disease [rarediseases.info.nih.gov]

Autosomal Recessive Spinocerebellar Ataxia 3

limbs Diminished vibratory sensation in the legs [ more ] 0002166 Mildly elevated creatine kinase 0008180 Nystagmus Involuntary, rapid, rhythmic eye movements 0000639 Optic [rarediseases.info.nih.gov]

Inability to coordinate movements when walking 0002066 Head tremor 0002346 Hearing impairment Deafness Hearing defect [ more ] 0000365 Impaired vibration sensation in the lower [rarediseases.info.nih.gov]

Charcot-Marie-Tooth Disease Type 1C

However, both of them had an evident bilateral pes cavus, generalized areflexia and decreased vibratory sense in the lower limbs. [bmcneurol.biomedcentral.com]

Both of them were asymptomatic (they did not complain about any motor or sensory disturbance in the upper or lower limbs). [bmcneurol.biomedcentral.com]

Spinocerebellar Ataxia with Axonal Neuropathy

sense in the lower limbs Demyelination of the posterior and lateral columns of the spinal cord Dysarthria Extensor plantar responses Gait ataxia Limb ataxia Mixed axonal [datagenno.com]

Craniofacial Ocular dysmetria General Onset after age 40 years Slow progression Neurologic Abnormality Cerebellar atrophy Cortical and subcortical atrophy Decreased vibratory [datagenno.com]

Syphilitic Arthritis

vibratory sense in his lower limbs. [medbullets.com]

[…] only Sorry, this question is for PEAK Premium Subscribers only Sorry, this question is for PEAK Premium Subscribers only (M1.MC.6) A 51-year-old man presents complaining of decreased [medbullets.com]

Hutchinson's Teeth

vibratory sense in his lower limbs. [step1.medbullets.com]

Autosomal Dominant Spastic Paraplegia Type 31

[…] type 7 is a form of hereditary spastic paraplegia (see this term) characterized by an onset usually in adulthood (but ranging from 10-72 years) of progressive bilateral lower [mendelian.co]

Friedreich Ataxia

absent lower limb reflexes, extensor plantar responses, dysarthria, and decreased vibratory sense and proprioception. [malacards.org]

[…] ataxia with associated limb muscle weakness, absent lower limb reflexes, extensor plantar responses, dysarthria, and decreased vibratory sense and proprioception. [flybase.org]

OMIM : 56 Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disorder characterized by progressive gait and limb ataxia with associated limb muscle weakness [malacards.org]